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PLoS Comput Biol ; 11(5): e1004096, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-26020786

RESUMEN

Whole-cell models that explicitly represent all cellular components at the molecular level have the potential to predict phenotype from genotype. However, even for simple bacteria, whole-cell models will contain thousands of parameters, many of which are poorly characterized or unknown. New algorithms are needed to estimate these parameters and enable researchers to build increasingly comprehensive models. We organized the Dialogue for Reverse Engineering Assessments and Methods (DREAM) 8 Whole-Cell Parameter Estimation Challenge to develop new parameter estimation algorithms for whole-cell models. We asked participants to identify a subset of parameters of a whole-cell model given the model's structure and in silico "experimental" data. Here we describe the challenge, the best performing methods, and new insights into the identifiability of whole-cell models. We also describe several valuable lessons we learned toward improving future challenges. Going forward, we believe that collaborative efforts supported by inexpensive cloud computing have the potential to solve whole-cell model parameter estimation.


Asunto(s)
Células/metabolismo , Modelos Biológicos , Algoritmos , Bacterias/genética , Bacterias/metabolismo , Bioingeniería , Nube Computacional , Biología Computacional , Simulación por Computador , Estudios de Asociación Genética/estadística & datos numéricos , Mutación , Mycoplasma genitalium/genética , Mycoplasma genitalium/metabolismo
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